Clinical Trials Directory

Trials / Completed

CompletedNCT02023151

Predicting the Clinical Response to Omalizumab With Anti-Immunoglobulin E (IgE) Ab Response or Syk Expression in Basophils

Predicting the Clinical Response to Omalizumab With Anti-IgE Response or Syk Expression in Basophils

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
17 (actual)
Sponsor
Johns Hopkins University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This research is being done to test whether differences in blood cells at baseline (start of the study) can be used to predict how well omalizumab will work in a patient. Omalizumab (Xolair) is a drug approved by the U.S. Food and Drug Administration (FDA) to treat asthma. Studies show that omalizumab improves the symptoms of asthma but some people experience better improvement than others.

Detailed description

From a therapeutic perspective, the study will determine whether changes in the peripheral blood basophil response to crosslinking anti-IgE Ab during treatment with omalizumab predicts the clinical efficacy of treatment with the drug. Secondary outcomes measures would focus on whether the starting level of anti-IgE-mediated histamine release, or the changes syk expression or its starting level would be sufficient to predict the clinical outcome. The study is a single-site trial to evaluate the utility of baseline basophil measures to predict the efficacy of subcutaneously administered omalizumab as an add-on therapy for the treatment of adult patients 18-75 years old who have been diagnosed with moderate to severe asthma according to current approved guidelines. Patients will be treated with omalizumab according to the standard FDA approved dosing table for a period of 16 weeks.

Conditions

Interventions

TypeNameDescription
DRUGOmalizumab

Timeline

Start date
2013-02-01
Primary completion
2016-06-01
Completion
2016-08-01
First posted
2013-12-30
Last updated
2017-12-11
Results posted
2017-12-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02023151. Inclusion in this directory is not an endorsement.